JP2003531129A - 炎症性腸疾患を治療するための抗体α４β７インテグリンおよびその使用 - Google Patents
炎症性腸疾患を治療するための抗体α４β７インテグリンおよびその使用Info
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- JP2003531129A JP2003531129A JP2001576078A JP2001576078A JP2003531129A JP 2003531129 A JP2003531129 A JP 2003531129A JP 2001576078 A JP2001576078 A JP 2001576078A JP 2001576078 A JP2001576078 A JP 2001576078A JP 2003531129 A JP2003531129 A JP 2003531129A
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Landscapes
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Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US55008200A | 2000-04-14 | 2000-04-14 | |
| US09/550,082 | 2000-04-14 | ||
| US09/748,960 US20010046496A1 (en) | 2000-04-14 | 2000-12-27 | Method of administering an antibody |
| US09/748,960 | 2000-12-27 | ||
| PCT/US2001/012234 WO2001078779A2 (en) | 2000-04-14 | 2001-04-13 | Antibody alpha4beta7 integrin and its use to treat inflammatory bowel disease |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
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| JP2012105379A Division JP5764524B2 (ja) | 2000-04-14 | 2012-05-02 | 炎症性腸疾患を治療するための抗体α４β７インテグリンおよびその使用 |
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| Publication Number | Publication Date |
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| JP2003531129A true JP2003531129A (ja) | 2003-10-21 |
| JP2003531129A5 JP2003531129A5 (enrdf_load_html_response) | 2011-02-17 |
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| JP2001576078A Withdrawn JP2003531129A (ja) | 2000-04-14 | 2001-04-13 | 炎症性腸疾患を治療するための抗体α４β７インテグリンおよびその使用 |
| JP2012105379A Expired - Lifetime JP5764524B2 (ja) | 2000-04-14 | 2012-05-02 | 炎症性腸疾患を治療するための抗体α４β７インテグリンおよびその使用 |
| JP2015007655A Expired - Lifetime JP6021959B2 (ja) | 2000-04-14 | 2015-01-19 | 炎症性腸疾患を治療するための抗体α４β７インテグリンおよびその使用 |
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| JP2015007655A Expired - Lifetime JP6021959B2 (ja) | 2000-04-14 | 2015-01-19 | 炎症性腸疾患を治療するための抗体α４β７インテグリンおよびその使用 |
Country Status (15)
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Families Citing this family (41)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TWI346558B (en) * | 2002-02-25 | 2011-08-11 | Elan Pharm Inc | Pharmaceutical composition for chronic treatment of inflammation and use thereof |
| GB0210121D0 (en) | 2002-05-02 | 2002-06-12 | Celltech R&D Ltd | Biological products |
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| DE602006017373D1 (de) * | 2005-07-08 | 2010-11-18 | Pfizer Ltd | Madcam-antikörper |
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| WO2007007152A2 (en) * | 2005-07-11 | 2007-01-18 | Pfizer Limited | Anti-madcam antibodies to treat metastatic cancers and chloroma |
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| JP2010521966A (ja) * | 2007-03-20 | 2010-07-01 | ミレニアム・ファーマシューティカルズ・インコーポレイテッド | α４β７インテグリンに結合するヒト化免疫グロブリンをコードする核酸 |
| US20110105724A1 (en) * | 2007-08-16 | 2011-05-05 | Stephanie Jane Clegg | Novel compounds |
| ES2751946T3 (es) * | 2009-03-20 | 2020-04-02 | Amgen Inc | Anticuerpo antagonista específico del heterodímero alfa-4-beta-7 |
| CA2807552A1 (en) | 2010-08-06 | 2012-02-09 | Moderna Therapeutics, Inc. | Engineered nucleic acids and methods of use thereof |
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| WO2012135805A2 (en) | 2011-03-31 | 2012-10-04 | modeRNA Therapeutics | Delivery and formulation of engineered nucleic acids |
| US9464124B2 (en) | 2011-09-12 | 2016-10-11 | Moderna Therapeutics, Inc. | Engineered nucleic acids and methods of use thereof |
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| AU2012340621B2 (en) * | 2011-11-23 | 2017-10-12 | Amgen Inc. | Administration of alpha4beta7 hetero-dimer-specific antibody |
| MX2014007233A (es) | 2011-12-16 | 2015-02-04 | Moderna Therapeutics Inc | Composiciones de nucleosidos, nucleotidos y acidos nucleicos modificados. |
| EA034583B1 (ru) * | 2012-01-12 | 2020-02-21 | Милленниум Фармасьютикалз, Инк. | ПРИМЕНЕНИЯ АНТИ-α4β7 АНТИТЕЛА |
| US9254311B2 (en) | 2012-04-02 | 2016-02-09 | Moderna Therapeutics, Inc. | Modified polynucleotides for the production of proteins |
| US9572897B2 (en) | 2012-04-02 | 2017-02-21 | Modernatx, Inc. | Modified polynucleotides for the production of cytoplasmic and cytoskeletal proteins |
| US9283287B2 (en) | 2012-04-02 | 2016-03-15 | Moderna Therapeutics, Inc. | Modified polynucleotides for the production of nuclear proteins |
| DE18200782T1 (de) | 2012-04-02 | 2021-10-21 | Modernatx, Inc. | Modifizierte polynukleotide zur herstellung von proteinen im zusammenhang mit erkrankungen beim menschen |
| WO2014081507A1 (en) | 2012-11-26 | 2014-05-30 | Moderna Therapeutics, Inc. | Terminally modified rna |
| US8980864B2 (en) | 2013-03-15 | 2015-03-17 | Moderna Therapeutics, Inc. | Compositions and methods of altering cholesterol levels |
| WO2015048744A2 (en) | 2013-09-30 | 2015-04-02 | Moderna Therapeutics, Inc. | Polynucleotides encoding immune modulating polypeptides |
| SG11201602503TA (en) | 2013-10-03 | 2016-04-28 | Moderna Therapeutics Inc | Polynucleotides encoding low density lipoprotein receptor |
| JP2017537105A (ja) | 2014-11-26 | 2017-12-14 | ミレニアム ファーマシューティカルズ， インコーポレイテッドＭｉｌｌｅｎｎｉｕｍ Ｐｈａｒｍａｃｅｕｔｉｃａｌｓ， Ｉｎｃ． | 瘻孔を伴うクローン病の治療用ベドリズマブ |
| EP3237004B1 (en) | 2014-12-24 | 2024-05-08 | Takeda Pharmaceutical Company Limited | Predicting outcome of treatment with an anti-alpha4 beta7 integrin antibody |
| CA3017743A1 (en) | 2016-03-14 | 2017-09-21 | Millennium Pharmaceuticals, Inc. | Method of preventing graft versus host disease |
| MA43755A (fr) | 2016-03-14 | 2018-11-28 | Millennium Pharm Inc | Méthodes de traitement ou de prévention d'une maladie du greffon contre l'hôte |
| US11760803B2 (en) | 2016-03-24 | 2023-09-19 | Takeda Pharmaceutical Company Limited | Methods of treating gastrointestinal immune-related adverse events in immune oncology treatments |
| TW201735949A (zh) | 2016-03-24 | 2017-10-16 | 千禧製藥公司 | 治療抗ctla4及抗pd-1組合治療中的胃腸道免疫相關不良事件之方法 |
| WO2017192867A1 (en) | 2016-05-04 | 2017-11-09 | Millennium Pharmaceuticals, Inc. | Triple combination therapy for treating inflammatory bowel disease |
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Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1998006248A2 (en) * | 1996-08-15 | 1998-02-19 | Leukosite, Inc. | HUMANIZED IMMUNOGLOBULIN REACTIVE WITH α4β7 INTEGRIN |
Family Cites Families (34)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4172124A (en) | 1978-04-28 | 1979-10-23 | The Wistar Institute | Method of producing tumor antibodies |
| GB8308235D0 (en) | 1983-03-25 | 1983-05-05 | Celltech Ltd | Polypeptides |
| US4816567A (en) | 1983-04-08 | 1989-03-28 | Genentech, Inc. | Recombinant immunoglobin preparations |
| GB8422238D0 (en) | 1984-09-03 | 1984-10-10 | Neuberger M S | Chimeric proteins |
| GB8607679D0 (en) | 1986-03-27 | 1986-04-30 | Winter G P | Recombinant dna product |
| US5225539A (en) | 1986-03-27 | 1993-07-06 | Medical Research Council | Recombinant altered antibodies and methods of making altered antibodies |
| US4946778A (en) | 1987-09-21 | 1990-08-07 | Genex Corporation | Single polypeptide chain binding molecules |
| JP3101690B2 (ja) | 1987-03-18 | 2000-10-23 | エス・ビィ・２・インコーポレイテッド | 変性抗体の、または変性抗体に関する改良 |
| JPH02500329A (ja) | 1987-05-21 | 1990-02-08 | クリエイテイブ・バイオマリキユールズ・インコーポレーテツド | ターゲット化多機能蛋白質 |
| US5403919A (en) * | 1987-08-11 | 1995-04-04 | Board Of Trustees Of The Leland Stanford Junior University Stanford University | Method to control leukocyte extravasation |
| US5538724A (en) * | 1987-08-11 | 1996-07-23 | The Board Of Trustees For The Leland Stanford Junior Univ. | Method of control leukocyte extravasation |
| JP3095168B2 (ja) | 1988-02-05 | 2000-10-03 | エル． モリソン，シェリー | ドメイン‐変性不変部を有する抗体 |
| GB8823869D0 (en) | 1988-10-12 | 1988-11-16 | Medical Res Council | Production of antibodies |
| IL162181A (en) | 1988-12-28 | 2006-04-10 | Pdl Biopharma Inc | A method of producing humanized immunoglubulin, and polynucleotides encoding the same |
| US5530101A (en) * | 1988-12-28 | 1996-06-25 | Protein Design Labs, Inc. | Humanized immunoglobulins |
| US5859205A (en) * | 1989-12-21 | 1999-01-12 | Celltech Limited | Humanised antibodies |
| WO1991010741A1 (en) | 1990-01-12 | 1991-07-25 | Cell Genesys, Inc. | Generation of xenogeneic antibodies |
| US5770429A (en) | 1990-08-29 | 1998-06-23 | Genpharm International, Inc. | Transgenic non-human animals capable of producing heterologous antibodies |
| US5545806A (en) | 1990-08-29 | 1996-08-13 | Genpharm International, Inc. | Ransgenic non-human animals for producing heterologous antibodies |
| EP0519596B1 (en) | 1991-05-17 | 2005-02-23 | Merck & Co. Inc. | A method for reducing the immunogenicity of antibody variable domains |
| WO1994004679A1 (en) | 1991-06-14 | 1994-03-03 | Genentech, Inc. | Method for making humanized antibodies |
| ES2206447T3 (es) * | 1991-06-14 | 2004-05-16 | Genentech, Inc. | Anticuerpo humanizado para heregulina. |
| WO1993006213A1 (en) | 1991-09-23 | 1993-04-01 | Medical Research Council | Production of chimeric antibodies - a combinatorial approach |
| US5871734A (en) * | 1992-01-13 | 1999-02-16 | Biogen, Inc. | Treatment for asthma with VLA-4 blocking agents |
| US5932214A (en) * | 1994-08-11 | 1999-08-03 | Biogen, Inc. | Treatment for inflammatory bowel disease with VLA-4 blockers |
| DK0682529T4 (da) * | 1993-02-09 | 2006-05-15 | Biogen Idec Inc | Antistof til behandling af insulinkrævende diabetes |
| DE614989T1 (de) | 1993-02-17 | 1995-09-28 | Morphosys Proteinoptimierung | Verfahren für in vivo Selektion von Ligandenbindende Proteine. |
| AU691811B2 (en) | 1993-06-16 | 1998-05-28 | Celltech Therapeutics Limited | Antibodies |
| US5840299A (en) | 1994-01-25 | 1998-11-24 | Athena Neurosciences, Inc. | Humanized antibodies against leukocyte adhesion molecule VLA-4 |
| GB2292079B (en) * | 1994-08-12 | 1998-07-15 | Flexpharm Ltd | Coated prednisolone preparation for the treatment of inflamatory bowel disease |
| US6551593B1 (en) * | 1995-02-10 | 2003-04-22 | Millennium Pharmaceuticals, Inc. | Treatment of Inflammatory bowel disease by inhibiting binding and/or signalling through α 4 β 7 and its ligands and madcam |
| US6015662A (en) * | 1996-01-23 | 2000-01-18 | Abbott Laboratories | Reagents for use as calibrators and controls |
| CA2722378C (en) | 1996-12-03 | 2015-02-03 | Amgen Fremont Inc. | Human antibodies that bind tnf.alpha. |
| CZ302997B6 (cs) * | 1998-09-14 | 2012-02-15 | Board Of Regents, The University Of Texas System | Použití protilátky nebo jejího fragmentu vázajícího antigen pro výrobu farmaceutického prípravku |
-
2000
- 2000-12-27 US US09/748,960 patent/US20010046496A1/en not_active Abandoned
-
2001
- 2001-04-13 AU AU2001251629A patent/AU2001251629A1/en not_active Abandoned
- 2001-04-13 EP EP10010997.4A patent/EP2298348B9/en not_active Expired - Lifetime
- 2001-04-13 ES ES01925028T patent/ES2398096T3/es not_active Expired - Lifetime
- 2001-04-13 PT PT100109974T patent/PT2298348T/pt unknown
- 2001-04-13 WO PCT/US2001/012234 patent/WO2001078779A2/en active Application Filing
- 2001-04-13 MX MXPA02010059A patent/MXPA02010059A/es active IP Right Grant
- 2001-04-13 DK DK10010997.4T patent/DK2298348T3/en active
- 2001-04-13 EP EP01925028A patent/EP1278543B1/en not_active Expired - Lifetime
- 2001-04-13 ES ES10010997.4T patent/ES2609689T3/es not_active Expired - Lifetime
- 2001-04-13 DK DK01925028.1T patent/DK1278543T3/da active
- 2001-04-13 JP JP2001576078A patent/JP2003531129A/ja not_active Withdrawn
- 2001-04-13 CA CA2406220A patent/CA2406220C/en not_active Expired - Lifetime
- 2001-04-13 EP EP16191558.2A patent/EP3167902B1/en not_active Revoked
-
2003
- 2003-12-15 US US10/735,863 patent/US20050095238A1/en not_active Abandoned
-
2011
- 2011-08-05 US US13/204,139 patent/US20120034243A1/en not_active Abandoned
-
2012
- 2012-05-02 JP JP2012105379A patent/JP5764524B2/ja not_active Expired - Lifetime
- 2012-12-18 CY CY20121101236T patent/CY1113489T1/el unknown
-
2014
- 2014-02-03 US US14/171,161 patent/US20140186345A1/en not_active Abandoned
- 2014-11-11 NL NL300702C patent/NL300702I1/nl unknown
- 2014-11-13 FR FR14C0080C patent/FR14C0080I2/fr active Active
- 2014-11-17 CY CY2014046C patent/CY2014046I1/el unknown
-
2015
- 2015-01-19 JP JP2015007655A patent/JP6021959B2/ja not_active Expired - Lifetime
-
2017
- 2017-01-05 CY CY20171100013T patent/CY1118429T1/el unknown
- 2017-04-11 LU LU00014C patent/LUC00014I2/fr unknown
- 2017-04-11 BE BE2017C009C patent/BE2017C009I2/nl unknown
-
2018
- 2018-11-02 US US16/179,157 patent/US20200002423A1/en not_active Abandoned
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1998006248A2 (en) * | 1996-08-15 | 1998-02-19 | Leukosite, Inc. | HUMANIZED IMMUNOGLOBULIN REACTIVE WITH α4β7 INTEGRIN |
Non-Patent Citations (2)
| Title |
|---|
| JPN5002028637; ＧＯＲＤＯＮ ＦＩＯＮＡ Ｈ: ＧＡＳＴＲＯＥＮＴＥＲＯＬＯＧＹ Ｖｏｌ．１１６ Ｎｏ．４ ＰＡＲＴ．２, 199904, ｐ．Ａ７２６ * |
| JPN5002028638; ＧＯＲＤＯＮ ＦＩＯＮＡ Ｈ: ＧＡＳＴＲＯＥＮＴＥＲＯＬＯＧＹ Ｖｏｌ．１１６ Ｎｏ．４ ＰＡＲＴ．２, 199904, ｐ．Ａ７２６ * |
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| JP2022132430A (ja) * | 2011-05-02 | 2022-09-08 | ミレニアム ファーマシューティカルズ， インコーポレイテッド | 抗α４β７抗体のための製剤 |
| JP7258941B2 (ja) | 2011-05-02 | 2023-04-17 | ミレニアム ファーマシューティカルズ， インコーポレイテッド | 抗α４β７抗体のための製剤 |
| JP2023076616A (ja) * | 2011-05-02 | 2023-06-01 | ミレニアム ファーマシューティカルズ， インコーポレイテッド | 抗α４β７抗体のための製剤 |
| JP7492057B2 (ja) | 2011-05-02 | 2024-05-28 | ミレニアム ファーマシューティカルズ， インコーポレイテッド | 抗α４β７抗体のための製剤 |
| JP2024098027A (ja) * | 2011-05-02 | 2024-07-19 | ミレニアム ファーマシューティカルズ， インコーポレイテッド | 抗α４β７抗体のための製剤 |
| JP7636651B2 (ja) | 2011-05-02 | 2025-02-27 | 武田薬品工業株式会社 | 抗α４β７抗体のための製剤 |
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